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In the Prescription Only Medicines (Human Use) Order 1997 , in article 1 (citation, commencement and interpretation), in paragraph (2)— (a) in the definition of “Community marketing authorization”, after “Council Regulation (EEC) No. 2309/93 ”, insert “or Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency”, and (b) in the definition of “United Kingdom marketing authorization” after “Schedule 6 to those Regulations” insert “or an authorization granted by the licensing authority in accordance with Article 126a of Directive 2001/83/EC ”;